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1 Ergebnisse
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KCTD7 deficiency defines a distinct neurodegenerative disor..:
Metz, Kyle A.
;
Teng, Xinchen
;
Coppens, Isabelle
...
Annals of Neurology. 84 (2018) 5 - p. 766-780 , 2018
Link:
https://doi.org/10.1002/ana.25351
RT Journal T1
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ana.25351&Exemplar=1&LAN=DE A1 Metz, Kyle A. A1 Teng, Xinchen A1 Coppens, Isabelle A1 Lamb, Heather M. A1 Wagner, Bart E. A1 Rosenfeld, Jill A. A1 Chen, Xianghui A1 Zhang, Yu A1 Kim, Hee Jong A1 Meadow, Michael E. A1 Wang, Tim Sen A1 Haberlandt, Edda D. A1 Anderson, Glenn W. A1 Leshinsky‐Silver, Esther A1 Bi, Weimin A1 Markello, Thomas C. A1 Pratt, Marsha A1 Makhseed, Nawal A1 Garnica, Adolfo A1 Danylchuk, Noelle R. A1 Burrow, Thomas A. A1 Jayakar, Parul A1 McKnight, Dianalee A1 Agadi, Satish A1 Gbedawo, Hatha A1 Stanley, Christine A1 Alber, Michael A1 Prehl, Isabelle A1 Peariso, Katrina A1 Ong, Min Tsui PB Wiley YR 2018 SN 0364-5134 SN 1531-8249 JF Annals of Neurology VO 84 IS 5 SP 766 OP 780 LK http://dx.doi.org/https://doi.org/10.1002/ana.25351 DO https://doi.org/10.1002/ana.25351 SF ELIB - SuUB Bremen
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